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EP1443130A1 - Film mince monocristallin homologue a super-reseau naturel, procede de preparation et dispositif dans lequel est utilise ledit film mince monocristallin - Google Patents

Film mince monocristallin homologue a super-reseau naturel, procede de preparation et dispositif dans lequel est utilise ledit film mince monocristallin Download PDF

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EP1443130A1
EP1443130A1 EP20020779976 EP02779976A EP1443130A1 EP 1443130 A1 EP1443130 A1 EP 1443130A1 EP 20020779976 EP20020779976 EP 20020779976 EP 02779976 A EP02779976 A EP 02779976A EP 1443130 A1 EP1443130 A1 EP 1443130A1
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zno
thin film
crystal
film
complex oxide
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EP1443130B1 (fr
EP1443130A4 (fr
Inventor
Hideo Hosono
Hiromichi Ota
Masahiro Orita
Kazushige Ueda
Masahiro Hirano
Toshio Room 207 Monarch Mizonokuchi KAMIYA III
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Hoya Corp
Japan Science and Technology Agency
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Japan Science and Technology Agency
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Priority claimed from JP2002266012A external-priority patent/JP4164562B2/ja
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Publication of EP1443130A1 publication Critical patent/EP1443130A1/fr
Publication of EP1443130A4 publication Critical patent/EP1443130A4/fr
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    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
    • H10D30/00—Field-effect transistors [FET]
    • H10D30/60—Insulated-gate field-effect transistors [IGFET]
    • H10D30/67—Thin-film transistors [TFT]
    • H10D30/674—Thin-film transistors [TFT] characterised by the active materials
    • H10D30/6755—Oxide semiconductors, e.g. zinc oxide, copper aluminium oxide or cadmium stannate
    • C—CHEMISTRY; METALLURGY
    • C30—CRYSTAL GROWTH
    • C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B23/00—Single-crystal growth by condensing evaporated or sublimed materials
    • C30B23/02—Epitaxial-layer growth
    • C—CHEMISTRY; METALLURGY
    • C30—CRYSTAL GROWTH
    • C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/10—Inorganic compounds or compositions
    • C30B29/16—Oxides
    • C30B29/22—Complex oxides
    • C—CHEMISTRY; METALLURGY
    • C30—CRYSTAL GROWTH
    • C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/60—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape characterised by shape
    • C30B29/68—Crystals with laminate structure, e.g. "superlattices"
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
    • H10D30/00—Field-effect transistors [FET]
    • H10D30/60—Insulated-gate field-effect transistors [IGFET]
    • H10D30/67—Thin-film transistors [TFT]
    • H10D30/6729—Thin-film transistors [TFT] characterised by the electrodes
    • H10D30/6737—Thin-film transistors [TFT] characterised by the electrodes characterised by the electrode materials
    • H10D30/6739—Conductor-insulator-semiconductor electrodes
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
    • H10D30/00—Field-effect transistors [FET]
    • H10D30/60—Insulated-gate field-effect transistors [IGFET]
    • H10D30/67—Thin-film transistors [TFT]
    • H10D30/674—Thin-film transistors [TFT] characterised by the active materials
    • H10D30/6755—Oxide semiconductors, e.g. zinc oxide, copper aluminium oxide or cadmium stannate
    • H10D30/6756—Amorphous oxide semiconductors
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
    • H10D64/00—Electrodes of devices having potential barriers
    • H10D64/60—Electrodes characterised by their materials
    • H10D64/62—Electrodes ohmically coupled to a semiconductor
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
    • H10D99/00—Subject matter not provided for in other groups of this subclass

Definitions

  • the present invention relates to a ZnO-based complex-oxide epitaxial single-crystal thin film having a natural superlattice structure, a production method of the single-crystal thin film, and a device, such as optical devices, electronic devices and X-ray optical devices, using the single-crystal thin film.
  • the term "superlattice” generically means a structure formed by orderly superimposing a number of ultra-thin crystal layers consisting of different materials.
  • the superlattice includes a "natural superlattice” based on periodicity in material's own crystal structure, and an “artificial superlattice” artificially created by alternately laminating ultra-thin films of different compositions.
  • periodic crystal layers or thin-film layers different in chemical composition and/or layer thickness can be variously combined to obtain specific characteristics different from the properties of a mixed crystal formed by combining layers consisting of the same material or by combining uniform layers. These specific characteristics mostly arise from the quantum size effect.
  • the quantum effect in a superlattice structure can be obtained only if each of the above thin films has a thickness of about 5 nm or less, which is less than the de Broglie wavelength of an electron. If each of the thin films has a thickness greater than this value, their semiconductive properties will be maintained as-is, or the interface between the thin films will merely act as a pure boundary condition. Whereas, when the film thickness becomes less than the de Broglie wavelength, electrons start behaving like waves to create new properties. This effect is generally referred to as "quantum size effect".
  • Electronic optical properties peculiar to a semiconductor crystal are based on a structure in which atoms are orderly arranged on a crystal lattice to induce a periodic potential to electrons.
  • a semiconductor superlattice has a long-periodic potential based on its superlattice structure. The movement of electrons under the synergistic action of the two potentials is believed to allow the superlattice to have new properties different from bulk crystals.
  • the superlattice structure exhibits characteristics of higher electron drift velocity, increased tunnel current based on the resonant tunneling effect, and enhanced luminescence efficiency based on the coupling between an electron and a hole.
  • a superlattice structure using a compound semiconductor material has already been put to practical use as devices including a high electron mobility transistor (HEMT) and semiconductor lasers for a communications or optical-disk.
  • HEMT high electron mobility transistor
  • the resonant tunneling effect can be utilized to obtain a specific current-voltage characteristic having negative differential-resistance.
  • a typical example utilizing the negative differential-resistance is a monostable-bistable transition logic element (MOBILE).
  • a field-effect transistor is an electronic device currently having the widest range of practical applications, such as unitary electronic elements of a semiconductor memory integrated circuit, high-frequency signal amplifying devices and liquid-crystal driving devices.
  • HEMET is one type of FETs, which uses a superlattice structure as an electron drift layer.
  • a silicon semiconductor compound is most widely used as their material in general. Specifically, a silicon single crystal is used for elements requiring high-speed operation, such as high-frequency signal amplifying devices or integrated circuit elements.
  • silicon cannot be used as the material of an ultra high-speed operation device or ultra high-frequency amplifying device, such as HEMT utilizing the quantum effect, because any superlattice structure suitable for silicon has not been developed.
  • amorphous silicon is used therefore in view of the need for larger-area plat-panel displays.
  • the artificial superlattice structure is prepared by epitaxially growth of two or more different semiconductors layers through various thin-film growth technologies.
  • epitaxial growth means that, in the state after a single-crystal thin film is grown on a single-crystal substrate, the respective crystal orientations of the thin film and the substrate are matched with one another.
  • the epitaxial growth can provide substrate/thin-film and thin-film/thin-film interfaces which are abrupt, and low in defect density.
  • a typical epitaxial thin-film growth technology includes a sputtering, a molecular beam epitaxy (MBE) and a chemical vapor deposition.
  • a sputtering process using thermal nonequilibrium vaporization is currently the most common technology, which is also industrially used.
  • a sputtering process for use in a film forming method utilizes a so-called sputtering-phenomenon of materials by high energy particles.
  • the sputtering phenomenon was discovered by W. Grove in 1852.
  • the sputtering phenomenon means that high-kinetic energy particles emitted onto the surface of a target (ions or atoms neutralized by electrons around the target surface) give the kinetic momentum of the particles to constitutive atoms of the target through elastic collision, and the recoil atoms are finally released from the target surface after repeatedly colliding with adjacent atoms.
  • the film forming method based on the sputtering process is intended to deposit the released constitutive atoms of the target on a substrate so as to form a thin film.
  • the sputtering process is not suitable for the preparation of an artificial superlattice, because it has a relatively high film-deposition speed.
  • the molecular beam epitaxy (MBE) process is a thin-film crystal growth technology named in 1968 by J. R. Arthur who was in Bell Laboratories at the time, and developed for compound semiconductors, primarily GaAs.
  • the MBE process can be considered as an improved or progressive type of a vacuum deposition process.
  • the MBE process is intended to perform an epitaxial crystal growth under the conditions that the flow of neutral molecules (or atoms) serving as raw materials of a crystal to be grown, or the intensity of a molecular beam (atomic beam), is accurately controlled in ultra-high vacuum, and the neutral molecules (or atoms) are deposited onto an accurately heated substrate.
  • the MBE process can be used for a wide range of materials including compound semiconductors, elementary semiconductors, such as Si, and various metal or oxide superconductors.
  • the difference from the conventional vacuum deposition process is in that (i) the vacuum degree in a growth chamber is set at 10 -7 ⁇ 10 -8 Pa or less, (ii) the crystal growth is performed while stably maintaining the cleanness of the crystal surface at the atomic scale, and (iii) the intensity of the molecular beam (atomic beam) is accurately controlled.
  • the MBE process is widely used in R&D and in production of commercial elements, such as HEMT.
  • the chemical vapor deposition (CVD) process is intended to grow a thin film having a given composition on a substrate by using chloride or organometal compound as a source material, and inducing the chemical reaction among source gases on the substrate.
  • the CVD process having excellent compatibility to mass production is used for producing practical devices, such as a superlattice structure for semiconductor lasers.
  • a compound-semiconductor superlattice structure is used to achieve a semiconductor laser with a lowered threshold current value and/or a improved stability of oscillation wavelength, and a higher-speed HEMT.
  • a GaN/InGaN/GaN superlattice and a ZnMgO/ZnO/ZnMgO superlattice have been proposed, and partly put to practical use.
  • Each of the layers in a superlattice structure has an extremely thin thickness of 1 to 100 atomic layers.
  • one of the layers locally has irregularity in thickness even at the atomic-layer level, such irregularity will have considerable adverse affects.
  • it is essential to control superlattice growth in the atomic-layer level through a sophisticated film-deposition technology, such as more advanced MBE process or CVD process. From this point of view, it is expected that if a superlattice existing in the natural is positively used instead of the aforementioned artificially prepared superlattice, a superlattice structure having an accurately controlled layer thickness can be prepared while simplifying the film-deposition process.
  • a natural superlattice structure has a potential for allowing one-dimensional superlattice structure (quantum wire structure) to be formed as well as two-dimensional superlattice structure (quantum well structure), and for allowing the range of applicable chemical compositions to be extended to oxides and others.
  • LuFeO 3 (ZnO) m is a natural superlattice having a LuO 1.5 layer and a FeO 1.5 (ZnO) m layer which are alternately laminated in the c-axis direction, wherein it has a rhombohedral structure when m is an odd number, and a hexagonal structure when m is an even number.
  • the value of m is the number of atomic layers of FeO 1.5 (ZnO) m
  • the crystal structure of LuFeO 3 (ZnO) m can be considered as a superlattice structure where the FeO 1.5 (ZnO) m layer having an atomic layer number of m and the LuO 1.5 layer having an atomic layer number of 1 are alternately laminated.
  • InGaO 3 (ZnO) m has a structure where Ga atoms are orderly arranged in ZnO when m > 7.
  • This group of compounds can be considered as a ZnO-based natural superlattice known as an ultraviolet-emitting material from the 1950s.
  • M' ions exist as periodic bands in the ZnO layer to allow the ZnO layer to have a one-dimensional superlattice structure (quantum wire structure).
  • a homologous-phases M 1 M 2 O 3 (ZnO) m thin film has been prepared by depositing source materials on a substrate heated at a high temperature through a sputtering process or a PLD process (H. Hiramatsu, W-S. Seo, and K. Koumoto, "Electrical and Optical Properties of Radio-Frequency-Sputtered Thin Films of (ZnO) 5 In 2 O 3 ", Chem. Mater. 10, 3033-3039 (1998)).
  • the above thin-film growth method for growing the homologous-phases M 1 M 2 O 3 (ZnO) m involves difficulties in adequately controlling the composition of a thin film to be formed, and in forming a homogeneous superlattice, due to significant vaporization in ZnO having a high vapor pressure. While the above thin-film growth method can be used to prepare an alignment film for liquid-crystal displays or the like, the quantum effect expecting from a superlattice structure cannot be fully obtained due to the heterogeneous superlattice structure.
  • the heterogeneous superlattice also means that the chemical composition ratio of the homologous phases is deviated from the stoichiometric ratio.
  • the deviation in the chemical composition ratio causes the occurrence of oxygen deficits in the homologous-phases and the generation of conduction carriers.
  • the homologous phases M 1 M 2 O 3 (ZnO) m thin film and ZnO thin film are transparent to visible light.
  • FETs using a compound semiconductor, such as silicon or GaAs have a sufficient performance for various purposes, they are opaque to visible light due to the optical characteristics of their materials, and therefore cannot serve as a transparent circuit.
  • the irradiation of visible light generates conduction carriers.
  • the irradiation of high-intensity light will cause the deterioration in characteristics of the transistor.
  • the pixels of the display has a relatively small open area ratio due to the opacity of the device to visible light.
  • the FET is irradiated with backlight illumination, a photoinduced current will be generated therein to cause the degradation of the switching characteristic.
  • the homologous-phases M 1 M 2 O 3 (ZnO) m or ZnO material having a large energy bandwidth can be used in place of the silicon or compound semiconductor to solve the above problems in the silicon and compound semiconductor field-effect transistors.
  • the present invention is directed to diffuse an element, such as Lu or Ga, into a ZnO single crystal or a ZnO epitaxial thin film serving as a base material so as to prepare a homologous M 1 M 2 O 3 (ZnO) m thin film phase, and then grow a single-crystal film from the thin film phase.
  • an element such as Lu or Ga
  • a natural-superlattice homologous single-crystal thin film comprising a complex oxide which is epitaxially grown on a ZnO epitaxial thin film.
  • the complex oxide is expressed by the following formula: M 1 M 2 O 3 (ZnO) m (wherein: M 1 is at least one selected from the group consisting of Ga, Fe, Sc, In, Lu, Yb, Tm, Er, Ho and Y; M 2 is at least one selected from the group consisting of Mn, Fe, Ga, In and Al; and m is a natural number of 1 or more).
  • a natural-superlattice homologous single-crystal thin film comprising a complex oxide which is epitaxially grown on a ZnO epitaxial thin film.
  • the ZnO epitaxial thin film is grown on a single-crystal substrate in advance of the growth of the complex oxide, and vanished during the growth of the complex oxide to allow the epitaxially grown complex oxide to reside directly on the single-crystal substrate.
  • the complex oxide is expressed by the following formula: M 1 M 2 O 3 (ZnO) m (wherein: M 1 is at least one selected from the group consisting of Ga, Fe, Sc, In, Lu, Yb, Tm, Er, Ho and Y; M 2 is at least one selected from the group consisting of Mn, Fe, Ga, In and Al; and m is a natural number of 1 or more).
  • a natural-superlattice homologous single-crystal thin film comprising a complex oxide which is epitaxially grown on a ZnO single crystal.
  • the complex oxide is expressed by the following formula: M 1 M 2 O 3 (ZnO) m (wherein: M 1 is at least one selected from the group consisting of Ga, Fe, Sc, In, Lu, Yb, Tm, Er, Ho and Y; M 2 is at least one selected from the group consisting of Mn, Fe, Ga, In and Al; and m is a natural number of 1 or more).
  • the difference of the m in the thickness direction of the thin film may be ⁇ 1 or less.
  • the m may be continuously changed in the thickness direction of the thin film.
  • the homologous single-crystal thin film set forth in either one of the first to third aspects of the present invention may include a surface region which has atomic level smoothness and an area of 0.5 ⁇ m ⁇ 0.5 ⁇ m.
  • a method of producing a natural-superlattice homologous single-crystal thin film comprises depositing on either one of a ZnO single crystal and a ZnO epitaxial thin film, an epitaxially grown complex oxide thin film expressed by the formula M 1 M 2 O 3 (ZnO) n (wherein: M 1 is at least one selected from the group consisting of Ga, Fe, Sc, In, Lu, Yb, Tm, Er, Ho and Y; M 2 is at least one selected from the group consisting of Mn, Fe, Ga, In and Al; and n is a natural number of 1 or more), and subjecting the deposited film to a thermal anneal treatment.
  • M 1 is at least one selected from the group consisting of Ga, Fe, Sc, In, Lu, Yb, Tm, Er, Ho and Y
  • M 2 is at least one selected from the group consisting of Mn, Fe, Ga, In and Al
  • n is a natural number of 1 or more
  • the thermal anneal treatment may be performed while covering the deposited film with a high-melting-point compound to prevent the vaporization of ZnO component from the deposited film.
  • the thermal anneal treatment may also be performed under the presence of ZnO vapor to prevent the vaporization of ZnO component from the deposited film.
  • an optical device an X-ray optical device or an electronic device, which comprises the homologous single-crystal thin film set forth in either one of the first to third aspects of the present invention.
  • a transparent-thin-film field-effect transistor comprising an active layer consisting of the homologous single-crystal thin film set forth in either one of the first to third aspects of the present invention.
  • the M 1 M 2 O 3 (ZnO) m is InMO 3 (ZnO) m , wherein M is at least one selected from the group consisting of In, Fe, Ga and Al, and m is an integer in the range of 1 to less than 50.
  • the homologous single-crystal thin film may be formed on a heat-resistant transparent oxide single-crystal substrate.
  • the homologous phases M 1 M 2 O 3 (ZnO) m single crystal thin film of the present invention is formed on a ZnO single crystal or a ZnO thin film epitaxially grown on a single-crystal substrate, such as an YSZ substrate or Al 2 O 3 substrate
  • a single-crystal substrate such as an YSZ substrate or Al 2 O 3 substrate
  • an element such as Lu or Ga
  • the ZnO epitaxial thin film is vanished, and the homologous phases M 1 M 2 O 3 (ZnO) m single-crystal thin film is epitaxially grown directly on the single-crystal substrate.
  • the layers of the superlattice have the same thickness or the same value of m, or are continuously changed in thickness or in the value of m.
  • the value of m or the thickness of natural superlattice can be controlled by changing the thickness of a thin film containing the element, such as Lu or Ga, or the temperature and/or time-period of the diffusion of the element, such as Lu or Ga, in the thin film.
  • the M 1 M 2 O 3 (ZnO) m is LuGa 3 (ZnO) m
  • the obtained homologous phases single-crystal thin film will have a wurtzite-type ZnO periodic, nano-wire structure or quantum dot structure. Based on these structures, an ultraviolet-emitting device or a quantum electronic device can be produced in the same manner as in an artificial superlattice structure.
  • the obtained homologous phases single-crystal thin film has a multi-step terrace-shaped surface morphology.
  • Each of the steps corresponds to the thickness of one of the layers of the superlattice.
  • the terrace has a surface with smoothness at the atomic level or an atomically smooth surface.
  • the homologous compound has a large thickness of one of two layers, and thus the grown thin film can have an atomically flat terrace having a width greater than 0.5 ⁇ m, which is greater than that of the substrate. In the homologous compound thin film having a larger value of m, the area of the atomically smooth surface can be further increased.
  • the atomically flat or smooth surface having a large area may be used as a sample tray for placing thereon a biological compound, such as DNA, to be observed using a tunneling electron microscope or a near-field optical microscope.
  • a biological compound such as DNA
  • the homologous compound having a low electrical resistance is suitable for this purpose.
  • the single crystal thin film of homologous compound containing ZnO as a primary component is transparent to visible light, and usable as a device constituting a transparent electronic circuit.
  • the thin-film field-effect transistor of the present invention uses this single crystal thin film as an active layer.
  • the homologous compound single crystal thin film can provide a new field-effect transistor having the following characteristics (1) to (3) superior to the conventional field-effect transistor using silicon.
  • a ZnO single-crystal thin film having an atomically smooth surface is epitaxially grown on a single crystal substrate, such as an YSZ substrate or Al 2 O 3 substrate, having an atomically smooth surface, through a MBE process, a pulsed laser deposition (PLD) process or other suitable film-forming process. If a ZnO single crystal is used, this step is unnecessary.
  • a single crystal substrate such as an YSZ substrate or Al 2 O 3 substrate, having an atomically smooth surface
  • PLD pulsed laser deposition
  • a thin film expressed by M 1 M 2 O 3 (ZnO) n is grown on the above ZnO thin film or a ZnO single crystal, through a MBE process, a pulsed laser deposition (PLD) process or other suitable film-forming process.
  • ZnO M 1 M 2 O 3
  • M 1 M 2 O 3 (ZnO) n is a natural number of 1 or more.
  • M 1 is at least one selected from the group consisting of Ga, Fe, Sc, In, Lu, Yb, Tm, Er, Ho and Y
  • M 2 is at least one selected from the group consisting of Mn, Fe, Ga, In and Al.
  • Each of Fe, Ga and In may be substituted for both M 1 and M 2 .
  • Fe, Ga and In forms homologous phases Fe 2 O 3 (ZnO) n , Ga 2 O 3 (ZnO) n and In 2 O 3 (ZnO) n , respectively.
  • the thin film obtained in this step is not essentially a single-crystal film, but may be a polycrystal or amorphous film.
  • the thin film is subjected to a thermal anneal treatment at a temperature in the range of 800°C to 1600°C.
  • the thermal anneal treatment is performed in a non-reducing atmosphere, preferably in the atmosphere.
  • the treatment temperature is set preferably in the range of 800°C to 1600°C, more preferably in the range of 1200°C to 1500°C. If the temperature is less than 800°C, the composition M 1 M 2 O 3 (ZnO) m will become heterogeneous due to reduced diffusion speed. If the temperature is greater than 1600°C, the composition M 1 M 2 O 3 (ZnO) m will also become heterogeneous due to vaporization of the ZnO component.
  • ZnO vapor may be added to the atmosphere to prevent the vaporization of the ZnO component.
  • a ZnO compound is added in a vessel for performing the treatment therein, at an amount capable of generating ZnO vapor corresponding to about 5% of the volume of the vessel.
  • the ZnO compound is in the form of powder or sintered compact.
  • the a thin film of a high-melting-point compound such as YSZ or Al 2 O 3 plate may be placed to cover over the film, an then the thermal anneal treatment may be performed in the atmosphere.
  • the thin film has a vertical surface area greater than the cross-sectional surface area thereof, the vertical surface may be covered with the high-melting-point compound thin plate. More preferably, the thin film is covered with the plate, and then subjected to the thermal anneal treatment in the atmosphere containing ZnO vapor.
  • the high-melting-point compound plate covering the surface of the thin film can prevent the ZnO powder from direct contact with the thin film.
  • the value of m in the M 1 M 2 O 3 (ZnO) m is a natural number of 1 or more, which is different from the value of n in the M 1 M 2 O 3 (ZnO) n , and is uniquely determined by the ratio of the thickness of the ZnO thin film to the thickness of the M 1 M 2 O 3 (ZnO) n thin film, as shown in Table 1.
  • the M 1 M 2 O 3 (ZnO) m single-crystal thin film will have a constant value of m in the thickness direction. If the composition after the anneal has a ZnO component less than that in the chemical composition specified by the value of m, the obtained single-crystal thin film will have a superlattice structure having m and m - 1 which are mixed up. Otherwise, if the composition after the anneal has a ZnO component greater than that in the chemical composition specified by the value of m, the obtained single-crystal thin film will have a superlattice structure having m and m + 1 which are mixed up.
  • the obtained single-crystal thin film will have a "chirped superlattice structure" in which the layers of the superlattice are changed in thickness spatially continuously.
  • the chirped superlattice structure can be used as a Bragg-diffraction grating capable of diffracting a wide range of wavelength.
  • the obtained single-crystal thin film can be considered as a superlattice structure having an M 2 O 1.5 • ZnO layer sandwiched by M 1 O 1.5 layers, and thereby the quantum effect is created in electrons residing in the M 2 O 1.5 • ZnO layer.
  • the obtained single-crystal thin film can be used as materials of an, optical device, such as light-emitting diodes and semiconductor lasers, and an electronic device, such as MOBILE, HEMT and FET, as with the artificial superlattice structures.
  • the thickness of the M 2 O 1.5 • ZnO layer in the obtained M 1 M 2 O 3 (ZnO) m thin film is 0.5 nm or more, the thickness can be controlled with an interval of 0.27 nm to allow the thin film to be used as the material of a mirror for reflecting X-ray.
  • a field-effect transistor according to the present invention will be described below in detail.
  • a heat-resistant transparent oxide single-crystal substrate such as a YSZ (yttria-stabilized zirconia), sapphire, MgO or ZnO substrate, is used as a substrate for the above homologous compound single-crystal thin film containing ZnO as a primary component.
  • a YSZ substrate which has a lattice constant close to the homologous compound containing ZnO and causes no chemical reaction with the compound at a temperature of 1400°C or less.
  • the substrate has a mean square surface roughness Rms of 1.0 nm or less.
  • the mean square surface roughness Rms can be calculated by scanning the surface, for example its area of 1 ⁇ m 2 , using an atom force microscope.
  • the oxide single-crystal substrate such as an YSZ substrate, may be heated at 1000°C or more in vacuum or the atmosphere to obtain an ultra-smoothed surface.
  • a structure reflecting the crystal structure of the oxide single-crystal appears on the ultra-smoothed surface.
  • this structure is generally referred to as atomically flattened or smoothed structure, which has terraces each having a width of about several hundred nm and steps each having a height of about sub-nanometer.
  • Each of the terraces is composed of atoms arrange on a plane, and is a fully smoothed surface except for a few defects existing thereon. However, in view of the entire substrate, it is not a fully smoothed surface due to the presence of the steps.
  • the structure When the structure is expressed by the roughness Rms based on the mean square surface roughness measurement method, it is 1.0 nm or less.
  • the roughness Rms is calculated by scanning the surface, for example its area of 1 ⁇ m 2 , using an atom force microscope.
  • a ZnO single-crystal thin film having an atomically smooth surface is epitaxially grown on the obtained atomically smooth surface of the heat-resistant transparent oxide substrate through a MBE process, pulsed, laser deposition (PLD) process or other suitable film-forming process.
  • PLD pulsed, laser deposition
  • the obtained thin film is not essentially a single-crystal film, but may be a polycrystal or amorphous film.
  • a high-melting-point compound plate such as YSZ or Al 2 O 3 is covered over the entire thin film, and then the thin film is subjected to a thermal anneal treatment at a high temperature of 1300°C or more in the atmosphere containing ZnO vapor.
  • the high-melting-point compound plate is used to cover over the thin film to prevent the contact between the after-mentioned ZnO powder and the surface of the thin film.
  • ZnO is filled in a vessel at an amount capable of generating ZnO vapor corresponding to 5 volume % or more relative to a reaction chamber.
  • the ZnO is in the form of powder or sintered compact.
  • the obtained single-crystal thin film can be considered as a superlattice structure having an MO 3 (ZnO) m' layer sandwiched by InO 1.5 layers, and thereby the quantum effect is created in electrons residing the interface between the MO 3 (ZnO) m' layer and the InO 1.5 layer.
  • the obtained single-crystal thin film can be used as the material of a high-frequency electronic device, as with the artificial superlattice structures.
  • a homologous single crystal thin film containing ZnO obtained through a reactive solid-phase epitaxy process has a composition close to the stoichiometric composition, and exhibits a high insulation performance of 10 8 ⁇ • cm or more at room temperature.
  • this single crystal thin film is suitable for a normally-off field-effect transistor.
  • the obtained homologous single-crystal thin film containing ZnO as a primary component is used as an active layer of a top-gate type metal-insulator-semiconductor (MIS) field-effect transistor.
  • MIS metal-insulator-semiconductor
  • a gate insulation film 3 and a metal film for a gate electrode 4 are first formed on a homologous ZnO-based single crystal thin film epitaxially grown on a substrate 1.
  • the gate insulation film 3 is preferably made of Al 2 O 3 .
  • the metal film for a gate electrode 4 may be made of Au, Ag, Al or Cu.
  • the field-effect transistor of the present invention is not limited to the top-gate type MIS field-effect transistor (MIS-FET), but may include other type of FET, such as a junction field-effect transistor (J-FET).
  • MIS-FET top-gate type MIS field-effect transistor
  • J-FET junction field-effect transistor
  • a ZnO thin film was grown on a YAS (111) single-crystal substrate (10 square mm ⁇ 0.5 mm t) at a substrate temperature of 800°C.
  • a KrF (248 nm) excimer laser was irradiated to a target of ZnO sintered body in a vacuum chamber set at an oxygen pressure of 3 ⁇ 10 -3 Pa to vaporize ZnO, and the ZnO was deposited on the YAS (111) single-crystal substrate heated at 800°C, at a deposition speed of 2 nm/min for 1 hour to form the ZnO thin film.
  • ZnO was deposited on the YSZ (111) substrate in (0001) orientation at a tilt angle of 0.02 to 0.1 degrees. Further, through an In-plain measurement, it was verified that the ZnO was epitaxially grown adequately. The epitaxial relationship between the ZnO and the substrate was ZnO (11-20) // YSZ (1-10).
  • the ZnO thin film formed on the YSZ (111) substrate was used as a substrate to grow LuGaO 3 (ZnO) 9 thereon at a substrate temperature 600°C.
  • a KrF (248 nm) excimer laser was irradiated to a target of LuGaO 3 (ZnO) 9 sintered body in a vacuum chamber set at an oxygen pressure of 3 ⁇ 10 -3 Pa to vaporize LuGaO 3 (ZnO) 9 , and the LuGaO 3 (ZnO) 9 was deposited on the ZnO thin film formed on the YSZ (111) single-crystal substrate heated at 600°C, at a deposition speed of 2 nm/min for 30 minutes to form a LuGaO 3 (ZnO) 9 thin film.
  • the LuGaO 3 (ZnO) 9 thin film had a thickness of 60 nm.
  • the formed LuGaO 3 (ZnO) 9 thin film was composed of nano-size microcrystals, and therefore the crystallinity of the thin film could not be evaluated by an XRD measurement.
  • the LuGaO 3 (ZnO) 9 / ZnO / YSZ layered thin film formed in the above Section-2 was entirely covered by an YSZ single crystal (10 mm ⁇ 10 mm ⁇ 0.5 mm t) plate. Further, in order to prevent the vaporization of ZnO component having a high vapor pressure, about 2 g of ZnO powder (mean particle size: 1 ⁇ m) was put on the YSZ plate covering the 3 layer films. Then, the layered thin film was put into an aluminum pot of (SSA-S), and a lid of the pot was closed. Then, the layered thin film was subjected to a thermal anneal treatment at 1450°C in the atmosphere for 30 minutes. After the completion of the thermal anneal treatment, an obtained single-crystal thin layer was cooled to room temperature in the pot.
  • SSA-S aluminum pot of
  • FIG. 1 shows an out-of-plane XRD pattern. Strong diffraction peaks of (0001) face of LuGaO 3 (ZnO) 17 were observed together with a YSZ (111) peak. This shows that LuGaO 3 (ZnO) 17 (0001) has strongly oriented against YSZ (111). The tilt angle of LuGaO 3 (ZnO) 17 (0001) face was determined as 0.1 degree based on the measurement of rocking curve.
  • LuGaO 3 (ZnO) 17 thin film was epitaxially grown.
  • the epitaxial relationship therebetween is as follows: LuGaO 3 (ZnO) 17 (0001) // YSZ (111) LuGaO 3 (ZnO) 17 (11-20) // YSZ (1-10)
  • the distance between adjacent LuO 1.5 layers was determined as 5 nm based on an XRD measurement of the formed LuGaO 3 (ZnO) 17 single-crystal thin film.
  • AFM atomic force microscope
  • FIG. 2 a structure having flat terraces with atomic-level surface smoothness and steps with a height of about 5 nm was clearly observed.
  • the smooth surface region of the atomically smooth terrace has an area of 1 ⁇ m ⁇ 1 ⁇ m or more. This is one of evidences supporting that the formed LuGaO 3 (ZnO) 17 thin film is a single crystal.
  • FIG. 3 shows optical absorption spectra at 10 K and 300 K. For comparison, an optical absorption spectrum of a ZnO epitaxial thin film is also shown in FIG. 3.
  • the Third Harmonics (wavelength: 355 nm) of neodimium doped yttrium aluminum garnet (Nd: YAG) was irradiated onto the thin film to induce the luminescence.
  • the resulting luminescence was focused by a lens, and led to an optical fiber bundle.
  • the output light is introduced into a spectrometer, and then detected using a charge-coupled device (CCD).
  • FIG 4 shows photoluminescence spectra at 10 K and 300 K.
  • In was selected as M 1 M 2 , and grown on the ZnO epitaxial thin film formed in the manner described in Example 1 to form an In 2 O 3 thin film.
  • a KrF (248 nm) excimer laser was irradiated to a target of In 2 O 3 sintered body in a vacuum chamber set at an oxygen pressure of 3 ⁇ 10 -3 Pa to vaporize LuGaO 3 (ZnO) 9 , and the In 2 O 3 was deposited on the YSZ (111) single-crystal substrate heated at 600°C, at a deposition speed of 2 nm/min for 30 minutes to form the In 2 O 3 thin film.
  • the In 2 O 3 was heteroepitaxially grown on the ZnO thin film, and the epitaxial relationship therebetween was as follows: In 2 O 3 (111) // ZnO (0001) // YSZ (111) In 2 O 3 (110) // ZnO (11-20) // YSZ (1-10).
  • the formed bilayer thin film was subjected to a thermal anneal treatment at 1300°C in the atmosphere for 20 minutes, in the manner as described in Example 1.
  • a thermal anneal treatment at 1300°C in the atmosphere for 20 minutes, in the manner as described in Example 1.
  • the formation of an epitaxial thin film of In 2 O 3 (ZnO 3 ) 4 , In 2 O 3 (ZnO 3 ) 5 and In 2 O 3 (ZnO 3 ) 6 which were mixed up was confirmed through a HRXRD measurement.
  • a thin film was grown on an YSZ (111) single crystal substrate using a target of LuGaO 3 (ZnO) 5 at a substrate temperature of room temperature.
  • the thickness of the formed thin film determined by the measurement of X-ray reflectance was 200 nm. Through an XRD measurement, it was proved that the formed thin film is amorphous.
  • the composition of the thin film was determined through a fluorescent X-ray analysis. As a result, while the atomic ratio of Lu/Ga was 1, the atomic ratio of Zn/Lu was 3, or ZnO was reduced as compared with the composition of the target.
  • the formed amorphous thin film was crystallized by the annealing (1450°C, 30 minutes) described in Example 1.
  • the formation of LuGaO 3 (ZnO) 3 (0001) was proved through a HRXRD measurement.
  • a strong LuGaO 3 (ZnO) 3 (0001) diffraction peak was observed together with an YSZ (111) diffraction peak.
  • Their orientation was as follows: LuGaO 3 (ZnO) 3 (0001) // YSZ (111).
  • the tilt angle of the thin film determined through the measurement of rocking curve was about 1 degree. No in-plane orientation was observed in an in-plane measurement. Therefore, the formed thin film is a c-axis oriented LuGaO 3 (ZnO) 3 film but not a single crystal.
  • a thin film was grown on an YSZ (111) single crystal substrate through a PLD process using a target of LuGaO 3 (ZnO) 9 at a substrate temperature of 500 to 900°C.
  • the thickness of the formed thin film determined by the measurement of X-ray reflectance was reduced as the substrate temperature was increased.
  • the composition of the thin film was determined through a fluorescent X-ray analysis. As a result, while the atomic ratio of Lu/Ga was 1 at any growth temperature, the atomic ratio of Zn/Lu was apt to be reduced as the substrate temperature was increased.
  • a ZnO thin film having a thickness of 2 mm was epitaxially grown on a YSZ (111) single-crystal substrate through a PLD process at a substrate temperature of 700°C. Then, after the substrate temperature was reduced to room temperature, a polycrystal InGaO 3 (ZnO) 5 thin film having a thickness of 150 nm was deposited on the ZnO epitaxial thin film through a PLD process. The formed bilayer thin film was taken out to the atmosphere, and subjected to a thermal anneal treatment using an electric furnace at 1400°C in the atmosphere for 30 minutes. After the completion of the treatment, the treated film was cooled to room temperature.
  • the thin film subjected to the heating was a single crystal InGaO 3 (ZnO) 5 as shown in FIG 6.
  • the surface of the thin film was an atomically smooth surface having atomically smooth terraces and steps with a height of 2 nm, as shown in FIG. 7.
  • the formed InGaO 3 (ZnO) 5 thin film is an insulator.
  • the bandgap of the InGaO 3 (ZnO) 5 was calculated as about 3.3 eV based on an optical absorption spectrum measured at room temperature.
  • a top-gate type MISFET device was formed through a photolithography process.
  • Au was used as the material of source and drain electrodes and amorphous Al 2 O 3 was used as a gate insulation film.
  • a channel length and a channel width were 0.5 mm and 0.2 mm, respectively.
  • FIG. 8 shows a current-voltage characteristic of the MISFET measured at room temperature.
  • the natural-superlattice homologous single-crystal thin film of the present invention can be used in an optical device (light-emitting diodes, laser diodes), an electronic device (monostable-bistable transition logic element devices utilizing a negative differential-resistance based on the resonant tunneling effect, high electron mobility transistors: HEMT, field-effect transistors: FET) and an X-ray optical device (soft X-ray reflection mirrors).
  • an optical device light-emitting diodes, laser diodes
  • an electronic device monostable-bistable transition logic element devices utilizing a negative differential-resistance based on the resonant tunneling effect
  • high electron mobility transistors high electron mobility transistors: HEMT, field-effect transistors: FET
  • X-ray optical device soft X-ray reflection mirrors

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EP02779976A 2001-11-05 2002-10-31 Film mince monocristallin homologue a super-reseau naturel, procede de preparation et dispositif dans lequel est utilise ledit film mince monocristallin Expired - Lifetime EP1443130B1 (fr)

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JP2001340066A JP4298194B2 (ja) 2001-11-05 2001-11-05 自然超格子ホモロガス単結晶薄膜の製造方法。
JP2002266012A JP4164562B2 (ja) 2002-09-11 2002-09-11 ホモロガス薄膜を活性層として用いる透明薄膜電界効果型トランジスタ
JP2002266012 2002-09-11
PCT/JP2002/011404 WO2003040441A1 (fr) 2001-11-05 2002-10-31 Film mince monocristallin homologue a super-reseau naturel, procede de preparation et dispositif dans lequel est utilise ledit film mince monocristallin

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US7061014B2 (en) 2006-06-13
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EP1443130A4 (fr) 2009-06-03
WO2003040441A1 (fr) 2003-05-15

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